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Bufotenine acetate

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Identification
Molecular formula
C12H15N2O2
CAS number
297-95-4
IUPAC name
[2-(1H-indol-3-yl)-1-methyl-ethyl]ammonium;acetate
State
State

At room temperature, bufotenine acetate is typically found in a solid state. Due to its stability, it remains solid under standard storage conditions.

Melting point (Celsius)
147.00
Melting point (Kelvin)
420.15
Boiling point (Celsius)
267.00
Boiling point (Kelvin)
540.15
General information
Molecular weight
218.27g/mol
Molar mass
218.2780g/mol
Density
1.4700g/cm3
Appearence

Bufotenine acetate typically appears as a white to off-white crystalline powder. It may also be found in other forms such as fine crystals or granules, depending on the specific preparation and storage conditions.

Comment on solubility

Solubility of [2-(1H-indol-3-yl)-1-methyl-ethyl]ammonium;acetate

The solubility of [2-(1H-indol-3-yl)-1-methyl-ethyl]ammonium;acetate can be influenced by various factors, primarily its ionic nature. Here are some noteworthy points regarding its solubility characteristics:

  • Solvent Interaction: This compound is expected to be soluble in polar solvents due to its ionic ammonium and acetate components.
  • Hydrogen Bonding: The presence of the indole group may increase interactions such as hydrogen bonding with solvents, potentially enhancing solubility.
  • Temperature Dependence: Solubility often increases with temperature for ionic compounds, so higher temperatures could promote greater dissolution.
  • pH Sensitivity: The solubility may vary with pH; in lower pH environments, the ammonium ion can remain protonated, favoring solubility.

In summary, while [2-(1H-indol-3-yl)-1-methyl-ethyl]ammonium;acetate is likely to exhibit solubility in polar solvents, the exact solubility behavior can vary depending on environmental conditions such as temperature and pH. Experimentation is often necessary to determine the precise solubility profile in specific solvents.

Interesting facts

Interesting Facts about [2-(1H-indol-3-yl)-1-methyl-ethyl]ammonium;acetate

[2-(1H-indol-3-yl)-1-methyl-ethyl]ammonium;acetate is a fascinating compound that brings together the complex world of organic chemistry and biological activity. Here are several noteworthy points about this compound:

  • Indole Derivative: This compound contains an indole structure, which is well-known for its presence in many natural products and biological molecules. Indoles are often associated with the aromaticity and are key building blocks in pharmaceuticals.
  • Biological Significance: Compounds containing indole structures have been studied for their various biological activities, including anti-inflammatory and anticancer properties. This opens avenues for research into therapeutic applications.
  • Ammonium Group: The presence of the ammonium group in this compound can enhance its solubility in biological fluids, potentially influencing how it interacts within biological systems.
  • Acetate Role: The acetate moiety acts as a counterion, which can affect the stability and the bioavailability of the compound. Ionic compounds like this often demonstrate interesting behavior in solution.
  • In Research: Compounds of this nature are often the subject of investigation in medicinal chemistry. They can serve as lead compounds in the development of new drugs targeting a variety of conditions.

In conclusion, [2-(1H-indol-3-yl)-1-methyl-ethyl]ammonium;acetate is not just a chemical formula but a gateway to understanding complex interactions in biological systems. As researchers continue to explore such compounds, they potentially unlock the secrets to new therapeutic strategies.

Synonyms
alpha-Methyltryptamine acetate
5118-26-3
3-(2-Aminopropyl)indole, acetate
U14164E
INDOLE, 3-(2-AMINOPROPYL)-, ACETATE
alpha-Methyl-1H-indole-3-ethanamine monoacetate
1H-Indole-3-ethanamine, alpha-methyl-, monoacetate